Anthropometric measurements in Egyptian patients with osteogenesis imperfecta
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference33 articles.
1. Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta;Alanay;Am J Hum Genet,2010
2. Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta;Barnes;New Engl J Med,2006
3. A new look at osteogenesis imperfecta. A clinical, Radiological and biochemical study of forty-two patients;Bauze;J Bone Joint Surg Br,1975
4. Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfecta;Becker;Am J Hum Genet,2011
5. Genotype-phenotype correlations in autosomal dominant osteogenesis imperfecta;Ben Amor;J Osteoporos,2011
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1. The patient clinical journey and socioeconomic impact of osteogenesis imperfecta: a systematic scoping review;Orphanet Journal of Rare Diseases;2023-02-22
2. Anthropometrics of Polish children with osteogenesis imperfecta: a single-centre retrospective cohort study;BMC Pediatrics;2022-10-06
3. Functional Independence of Taiwanese Children with Osteogenesis Imperfecta;Journal of Personalized Medicine;2022-07-24
4. Finite Element Analysis of 3D Models of Upper and Lower Limbs of Mexican Patients with Osteogenesis Imperfecta (OI) Type III;Advanced Structured Materials;2019-06-27
5. Calcium intake improvement after nutritional intervention in paediatric patients with osteogenesis imperfecta;Journal of Human Nutrition and Dietetics;2019-04-29
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